Cas 134673-10-2,4-nitro-N-[1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-en-3-yl]benzamide

134673-10-2

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Basic information

Product Name: 4-nitro-N-[1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-en-3-yl]benzamide
Synonyms: 4-nitro-N-[1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-en-3-yl]benzamide
CAS NO:134673-10-2
Molecular Formula: C₂₅H₃₄N₂O₄
Molecular Weight: 426.54846
EINECS: N/A
Product Categories: N/A
Mol File: 134673-10-2.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-nitro-N-[1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-en-3-yl]benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-nitro-N-[1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-en-3-yl]benzamide(134673-10-2)
EPA Substance Registry System: 4-nitro-N-[1-hydroxy-5,5,9,11,11-pentamethyltricyclo[7.3.1.0~2,7~]tridec-2(7)-en-3-yl]benzamide(134673-10-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 134673-10-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134673-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,6,7 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 134673-10:
(8*1)+(7*3)+(6*4)+(5*6)+(4*7)+(3*3)+(2*1)+(1*0)=122
122 % 10 = 2
So 134673-10-2 is a valid CAS Registry Number.

134673-10-2Upstream product

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134673-10-2Relevant academic research and scientific papers

Diisophorone and Related Compounds, Part 29. 3-Aminodiisophorane Derivatives

Kurzer, Frederick,Patel, Jayantilal N.

, p. 530 - 540 (2007/10/02)

3-Aminodiisophor-2(7)-en-1-ol and homologues are obtained from the readily accessible 3-ketones by reduction of their respective ketoximes, and are characterized as suitable derivatives.The 3-(ω-phenylthioureido) compound undergoes cyclodehydration to a substituted 8,11a-methanoncyclooctabenzthiazine.The structures of the individual compounds are correlated with their assigned 13C NMR spectra.

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